Surface glycans contribute to differences between seminal prostasomes from normozoospermic and oligozoospermic men

• Main Authors: Bojana Milutinović, Sanja Goč, Ninoslav Mitić, Maja Kosanović, Miroslava Janković
• Format: Article
• Language: English
• Published: Upsala Medical Society 2019-04-01
• Series: Upsala Journal of Medical Sciences
• Subjects: Glycosylation; prostasomes; seminal plasma; sialic acid
• Online Access: http://dx.doi.org/10.1080/03009734.2019.1592266

Background: Extracellular vesicles (EVs), released from the plasma membrane or intracellular compartments, have a specific composition related to their parent cells, but they can, additionally, be modified by the extracellular environment. Although glycans are known to contribute to EV composition and may have biomedical importance as biomarkers and recognition signals, they have not been extensively investigated. In this study, seminal prostasomes, i.e. EVs from seminal plasma (SP) of normo- and oligozoospermic men, were analyzed in order to detect possible changes in their surface glycans under altered physiological conditions. Methods: Prostasomes were isolated from pooled SP by differential centrifugation and gel filtration, followed by glycobiochemical characterization using lectin/immune-transmission microscopy and ion-exchange chromatography. Results: Within the frame of overall similarity in protein composition, surface glycans specifically contributed to the differences between the examined groups of prostasomes in terms of presentation of sialylated and mannosylated moieties. These changes did not affect their anti-oxidative capacity, but implied a possible influence on the accessibility of galectin-3 to its ligands on the prostasomal surface. Conclusions: Subtle differences in the presentation of surface molecules may be helpful for differentiation among vesicles sharing the same physical properties. In addition, this may point to some unexpected regulatory mechanisms of interaction of distinct populations of vesicles with their binding partners.